About this role
The LIMS Master Data Specialist is responsible for the creation, modification, maintenance, and verification of LIMS master data objects within LabWare. Working within the governance framework defined by the master data governance council, the Specialist handles requests from operational teams (analytical development and QC), executes master data builds for new products or methods, and serves as a subject matter expert (SME) for LIMS data during audits and operational troubleshooting.
- Strong experience with LabWare LIMS configuration, master data maintenance, workflow templates, and calculation scripting review
- Understanding of LIMS Basic scripting, SQL (preferred), Crystal Reports, ELN templates, and system interfaces (ERP/instrument integration)
- Knowledge of pharmaceutical QC workflows, analytical testing, and master data governance
- Ability to interpret analytical methods and translate them into structured LIMS configurations
- Detail-oriented, organized, and effective in managing multiple priorities with strong written communication and collaboration skills
- 3–6 years in QC, analytical development, regulatory, or laboratory informatics, including 1–2 years of direct LabWare LIMS configuration or master data management experience